A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv836



Internal ID15544771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37105053..37149088hg38UCSC Ensembl
Outerchr10:37393981..37438016hg19UCSC Ensembl
Outerchr10:37433987..37478022hg18UCSC Ensembl
Outerchr10:37433987..37478022hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3844036
hg1944036
hg1844036
hg1744036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7201
Supporting Variants
SamplesNA19240
Known GenesANKRD30A
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv836
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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